N,N-dimethyl glycine-promoted Ullmann coupling reaction of phenols and aryl halides

Dawei Ma; Qian Cai

doi:10.1021/ol0350947

N,N-dimethyl glycine-promoted Ullmann coupling reaction of phenols and aryl halides

Org Lett. 2003 Oct 16;5(21):3799-802. doi: 10.1021/ol0350947.

Authors

Dawei Ma¹, Qian Cai

Affiliation

¹ State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China. madw@pub.sioc.ac.cn

PMID: 14535713
DOI: 10.1021/ol0350947

Abstract

[reaction: see text] Ullmann-type diaryl ether synthesis can be performed at 90 degrees C using either aryl iodides or aryl bromides as the substrates under the assistance of N,N-dimethylglycine.

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Catalysis
Hydrocarbons, Halogenated / chemistry*
Models, Chemical
Molecular Structure
Phenols / chemistry*
Sarcosine / analogs & derivatives*
Sarcosine / chemistry*

Substances

Hydrocarbons, Halogenated
Phenols
dimethylglycine
Sarcosine